
An analysis of AERONET aerosol absorption properties and classifications representative of aerosol source regions
Author(s) -
Giles D. M.,
Holben B. N.,
Eck T. F.,
Sinyuk A.,
Smirnov A.,
Slutsker I.,
Dickerson R. R.,
Thompson A. M.,
Schafer J. S.
Publication year - 2012
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2012jd018127
Subject(s) - aeronet , aerosol , angstrom exponent , single scattering albedo , environmental science , absorption (acoustics) , atmospheric sciences , extinction (optical mineralogy) , radiative transfer , albedo (alchemy) , mineral dust , remote sensing , meteorology , chemistry , physics , mineralogy , geography , optics , art , performance art , art history
Partitioning of mineral dust, pollution, smoke, and mixtures using remote sensing techniques can help improve accuracy of satellite retrievals and assessments of the aerosol radiative impact on climate. Spectral aerosol optical depth ( τ ) and single scattering albedo ( ω o ) from Aerosol Robotic Network (AERONET) measurements are used to form absorption (i.e., ω o and absorption Ångström exponent ( α abs )) and size (i.e., extinction Ångström exponent ( α ext ) and fine mode fraction of τ ) relationships to infer dominant aerosol types. Using the long‐term AERONET data set (1999–2010), 19 sites are grouped by aerosol type based on known source regions to (1) determine the average ω o and α abs at each site (expanding upon previous work), (2) perform a sensitivity study on α abs by varying the spectral ω o , and (3) test the ability of each absorption and size relationship to distinguish aerosol types. The spectral ω o averages indicate slightly more aerosol absorption (i.e., a 0.0 < δω o ≤ 0.02 decrease) than in previous work, and optical mixtures of pollution and smoke with dust show stronger absorption than dust alone. Frequency distributions of α abs show significant overlap among aerosol type categories, and at least 10% of the α abs retrievals in each category are below 1.0. Perturbing the spectral ω o by ±0.03 induces significant α abs changes from the unperturbed value by at least ∼±0.6 for Dust, ∼±0.2 for Mixed, and ∼±0.1 for Urban/Industrial and Biomass Burning. The ω o440nm and α ext440–870nm relationship shows the best separation among aerosol type clusters, providing a simple technique for determining aerosol type from surface‐ and future space‐based instrumentation.